Basic Trial Information
Trial Description
     Summary
     Further Trial Information
     Eligibility Criteria
Trial Contact Information

Basic Trial Information

Trial Description

Summary

RATIONALE: Drugs used in chemotherapy such as doxorubicin and ifosfamide use different ways to stop tumor cells from dividing so they stop growing or die. Colony-stimulating factors, such as pegfilgrastim, cause the body to make blood cells. It is not yet known whether doxorubicin alone is more effective with or without ifosfamide and pegfilgrastim in treating soft tissue sarcoma.

PURPOSE: This randomized phase III trial is studying giving doxorubicin alone to see how well it works compared to giving doxorubicin together with ifosfamide and pegfilgrastim in treating patients with locally advanced or metastatic soft tissue sarcoma.

Further Study Information

OBJECTIVES:

• Compare the progression-free and overall survival of patients with locally advanced or metastatic soft tissue sarcoma treated with doxorubicin with vs without ifosfamide and pegfilgrastim as first-line therapy.

• Compare the response in patients treated with these regimens.

• Compare the treatment-related mortality of patients treated with these regimens.

• Compare the toxicity of these regimens in these patients.

OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to WHO performance status (0 vs 1), age group (less than 50 years of age vs 50 years of age and over), presence of liver metastases (yes vs no), histological grade (2 vs 3), and participating center. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive doxorubicin IV on day 1 (or IV continuously on days 1-3).

• Arm II: Patients receive doxorubicin IV on days 1-3 and ifosfamide IV over 4 hours on days 1-4. Patients also receive pegfilgrastim subcutaneously on day 5.

In both arms, treatment repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Patients are followed every 8 weeks until disease progression and then every 12 weeks thereafter.

PROJECTED ACCRUAL: A total of 450 patients will be accrued for this study within 4 years.

Eligibility Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed soft tissue sarcoma

• Locally advanced unresectable* OR metastatic disease

• High-grade (grade 2-3) disease according to the FNLCC grading system NOTE: *Disease that could prove resectable (including pulmonary metastasectomy) after a response to chemotherapy is allowed

• The following tumor types are eligible:

• Malignant fibrous histiocytoma

• Myxoid and round cell liposarcoma, pleomorphic liposarcoma, or dedifferentiated liposarcoma

• Pleomorphic rhabdomyosarcoma

• Synovial sarcoma

• Myxofibrosarcoma, intermediate and high-grade

• Fibrosarcoma

• Leiomyosarcoma

• Angiosarcoma

• Malignant peripheral nerve sheath tumor

• Epithelioid sarcoma

• Alveolar rhabdomyosarcoma

• Unclassifiable sarcoma, not otherwise specified

• The following tumor types are not eligible:

• Gastrointestinal stromal tumor

• Mixed mesodermal tumor

• Chondrosarcoma

• Malignant mesothelioma

• Neuroblastoma

• Osteosarcoma

• Ewing's sarcoma/primitive neuroectodermal tumor

• Desmoplastic small round cell tumor

• Embryonal rhabdomyosarcoma

• Alveolar soft part sarcoma

• Must have a measurable lesion with clinical evidence of progression within the past 6 weeks

• Osseous lesions and pleural effusions are not considered measurable

• No known or symptomatic CNS metastases

PATIENT CHARACTERISTICS:

Age

• 18 to 60

Performance status

• WHO 0-1

Life expectancy

• Not specified

Hematopoietic

• Absolute neutrophil count at least 2,000/mm^3

• Platelet count at least 100,000/mm^3

Hepatic

• Bilirubin no greater than 1.8 mg/dL

• Albumin at least 2.5 g/dL

Renal

• Creatinine no greater than 1.4 mg/dL OR

• Creatinine clearance greater than 65 mL/min

Cardiovascular

• No history of cardiovascular disease

Other

• Not pregnant

• Negative pregnancy test

• Fertile patients must use effective contraception

• No other severe medical illness

• No psychosis

• No other prior or concurrent malignancy except adequately treated carcinoma in situ of the cervix or basal cell skin cancer

• No psychological, familial, sociological, or geographical condition that would preclude study compliance and follow-up schedule

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• No prior chemotherapy for advanced or metastatic disease

• Prior adjuvant chemotherapy allowed provided there was no disease progression within 6 months after completion of treatment

Endocrine therapy

• Not specified

Radiotherapy

• No prior radiotherapy to the sole index lesion

Surgery

• Not specified

Trial Contact Information

Trial Lead Organizations/Sponsors

European Organization for Research and Treatment of Cancer

Ian Robert Judson

Link to the current ClinicalTrials.gov record.
NLM Identifer NCT00061984
Information obtained from ClinicalTrials.gov on December 20, 2011

Back to Top